Agfa Receives FDA 510(k) Clearance for DR 800 With Tomosynthesis
Agfa announces today that it has received FDA 510(k) clearance for its DR 800 multipurpose imaging system with tomosynthesis.
- Agfa announces today that it has received FDA 510(k) clearance for its DR 800 multipurpose imaging system with tomosynthesis.
- With the DR 800, Agfa moves from 2D single plane imaging to multi-slice image reconstruction.
- The DR 800 includes Agfa's brand-new, tomosynthesis algorithms for iterative reconstruction, which deliver images with less noise and fewer artefacts.
- "With the FDA 510(k) clearance for tomosynthesis, the DR 800 supports best-in-class multi-slice imaging, using algorithms that reconstruct images very quickly."